JPS6098525A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS6098525A
JPS6098525A JP58205946A JP20594683A JPS6098525A JP S6098525 A JPS6098525 A JP S6098525A JP 58205946 A JP58205946 A JP 58205946A JP 20594683 A JP20594683 A JP 20594683A JP S6098525 A JPS6098525 A JP S6098525A
Authority
JP
Japan
Prior art keywords
magnetic
org
group
organic dye
recording medium
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP58205946A
Other languages
Japanese (ja)
Other versions
JPH0262893B2 (en
Inventor
Hiromitsu Katsura
桂 宏光
Shigeyuki Ehashi
江橋 重行
Shuji Miyazaki
修次 宮崎
Michiji Hikosaka
彦坂 道迩
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Artience Co Ltd
Original Assignee
Toyo Ink SC Holdings Co Ltd
Toyo Ink Mfg Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyo Ink SC Holdings Co Ltd, Toyo Ink Mfg Co Ltd filed Critical Toyo Ink SC Holdings Co Ltd
Priority to JP58205946A priority Critical patent/JPS6098525A/en
Publication of JPS6098525A publication Critical patent/JPS6098525A/en
Publication of JPH0262893B2 publication Critical patent/JPH0262893B2/ja
Granted legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To improve dispersibility and magnetic characteristics of magnetic powder by incorporating an org. dye compd. having 1 or <=2 acidic groups or the salts thereof into a magnetic layer. CONSTITUTION:The acidic group refers to a hydroxyl group, carboxyl group, sulfonic acid group, etc. The org. dye compd. that can have these acidic groups is an azo compd., etc. The org. dye compd. has a substituent except the acidic group and the acid group may form a salt by a metal or org. amine, etc. The magnetic paint obtd. by using the org. dye compd. and kneading and dispersing magnetic powder and binder by using an org. solvent, etc. is excellent dispersion stability and a low viscosity. The paint decrease varinish sepn. with age, is easily dispersible again and has excellent workability for coating.

Description

【発明の詳細な説明】 本発明は磁性粉および結着剤を用いた磁気記録媒体に関
するもので、特に磁性粉の分散性および磁気特性を向上
させた磁気記録媒体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium using magnetic powder and a binder, and particularly to a magnetic recording medium in which the dispersibility and magnetic properties of the magnetic powder are improved.

従来、録音テープ、ビデオテープ、磁気ディスク、フロ
ッピーディスク等の磁気記録媒体にあっては、ポリエチ
レンテレフタレート、ポリエチレンナフタレート、三酢
酸セルロース、ポリカーボネート、ポリプロピレン、ポ
リ塩化ビニル、アルミニウム、合金などの支持体上に。
Conventionally, magnetic recording media such as audio tapes, video tapes, magnetic disks, and floppy disks have been prepared on supports such as polyethylene terephthalate, polyethylene naphthalate, cellulose triacetate, polycarbonate, polypropylene, polyvinyl chloride, aluminum, and alloys. To.

7−Fez03. Fe704L、コバルトをドープし
たγ−Fez03. CrO2,鉄粉および鉄−コバル
トーニソケルの合金等の磁性粉を、塩化ビニル−酢酸ビ
ニル共重合体、塩化ビニル−塩化ビニリデン共重合体、
ポリアクリル酸ブチル、アクリル酸ブヂルーアクリロニ
トリル共重合体、セルロース系樹脂、エポキシ系樹脂、
ポリウレタン系樹脂等の結着剤と混練して塗工していた
7-Fez03. Fe704L, cobalt-doped γ-Fez03. Magnetic powders such as CrO2, iron powders, and iron-cobalt nitride alloys are combined with vinyl chloride-vinyl acetate copolymers, vinyl chloride-vinylidene chloride copolymers,
Butyl acrylate, butyl acrylate-acrylonitrile copolymer, cellulose resin, epoxy resin,
It was applied by kneading it with a binder such as polyurethane resin.

しかしながら、これらの結着剤単独あるいは2種以上の
組合せによってもこれら結着剤中への磁性粉の分散性は
不良であるため2表面の平滑性、安定性等が不十分とな
り、さらに、磁気特性においても角型比(Br/8m)
 、 S/N比および感度等が非常に低かった。
However, even when using these binders alone or in combination of two or more, the dispersibility of magnetic powder in these binders is poor, resulting in insufficient smoothness and stability of the two surfaces. In terms of characteristics, the squareness ratio (Br/8m)
, S/N ratio, sensitivity, etc. were very low.

このため、磁性粉の分散性、安定性等を向上させる目的
で1種々の添加剤が使用されている。
For this reason, various additives are used for the purpose of improving the dispersibility, stability, etc. of magnetic powder.

例えば、高級脂肪酸、脂肪酸アミド、脂肪酸エステル、
4級アルコールエステル、ポリエチレンオキサイド、レ
シチン等である。
For example, higher fatty acids, fatty acid amides, fatty acid esters,
These include quaternary alcohol ester, polyethylene oxide, lecithin, etc.

しかし、これらの添加剤を加えても、かならずしも望ま
しい特性を有する磁性層を得ることは困難であった。例
えば、これらの添加剤を多量に使用した場合に2表面平
滑性、走行安定性はいくぶん改良されるが、磁性層の機
械的強度の低下、あるいは磁性層表面に添加剤がしみ出
てくる。いわゆるブルーミング現象が発生し。
However, even with the addition of these additives, it has been difficult to obtain a magnetic layer having desirable characteristics. For example, when a large amount of these additives is used, surface smoothness and running stability are improved to some extent, but the mechanical strength of the magnetic layer decreases or the additives seep out onto the surface of the magnetic layer. A so-called blooming phenomenon occurs.

磁気記録媒体として好ましくない結果を与える。このよ
うに、磁性層の特性および分散性も。
This gives undesirable results as a magnetic recording medium. In this way, the properties and dispersion of the magnetic layer as well.

けっして満足のいくものではなかった。It was by no means satisfactory.

本発明者等は、かかる欠点を改良すべく鋭意検討をした
結果1本発明をなすに至った。
The inventors of the present invention have made intensive studies to improve these drawbacks, and as a result, they have come up with the present invention.

すなわち9本発明は、磁性粉および結着剤を含む磁性層
を支持体上に形成して成る磁気記録媒体において、磁性
層に、酸性基またはその塩を1個または2個以上有する
有機色素化合物を含有せしめてなる磁気記録媒体に係わ
るものである。
That is, the present invention provides a magnetic recording medium in which a magnetic layer containing magnetic powder and a binder is formed on a support, wherein the magnetic layer contains an organic dye compound having one or more acidic groups or salts thereof. The present invention relates to a magnetic recording medium containing the following.

本発明に用いられる酸性基を有する有機色素化合物にお
いて、酸性基とは、水酸基、カルボキシル基、スルホン
酸基等であり、また、これら酸性基を持ち得る有機色素
化合物は、アゾ化合物2例えば、β−ナフトール系、β
−オキシナフトエ酸系、β−オキシナフトエ酸アリリド
系、アセト酢酸アリリド系、アセト酢酸アミノベンズイ
ミダシロン系、ピラゾロン系または縮合アゾ系、縮合多
環化合物9例えば、フタロシアニン系、キナクリドン系
、アントラキノン系、ペリレン系、ペリノン系、チオイ
ンジゴ系。
In the organic dye compound having an acidic group used in the present invention, the acidic group is a hydroxyl group, a carboxyl group, a sulfonic acid group, etc., and the organic dye compound that can have these acidic groups is an azo compound 2, for example, β −Naphthol series, β
- Oxynaphthoic acid series, β-oxynaphthoic acid arylide series, acetoacetic acid allylide series, acetoacetic acid aminobenzimidacylon series, pyrazolone series or fused azo series, fused polycyclic compounds 9 For example, phthalocyanine series, quinacridone series, anthraquinone series , perylene series, perinone series, thioindigo series.

ジオキサジン系、イソインドリノン系、キノフタロン系
またはトリフェニルメタン系、金属錯体化合物、に例え
ば、アゾ系、ニトロソ系及びアゾメチン系、また、これ
ら化合物は金属と錯体を形成していない配位子のままで
も良い。または、染付はレーキ化合物2例えば、酸性染
料レーキ系、塩基性染料レーキ系等である。酸性基は上
記有機色素化合物に直接結合するか、あるいは、カルボ
ン酸アミド、または、スルホン酸アミドを介し、もしく
は介さない置換されていても良い炭素数1〜20の飽和
もしくは不飽和のアルキレン基またはアリレン基を介し
て結合していても良い。
Dioxazine series, isoindolinone series, quinophthalone series or triphenylmethane series, metal complex compounds, such as azo series, nitroso series and azomethine series, and these compounds remain as ligands that do not form complexes with metals. But it's okay. Alternatively, dyeing may be done using a lake compound 2, such as an acidic dye lake system or a basic dye lake system. The acidic group is directly bonded to the organic dye compound, or is an optionally substituted saturated or unsaturated alkylene group having 1 to 20 carbon atoms, with or without a carboxylic acid amide or sulfonic acid amide. They may be bonded via an arylene group.

また2本発明の有機色素化合物は酸性基以外に、炭素数
1〜20の飽和もしくは不飽和アルキル基、了り−ル基
、ハロゲン原子、−OR+。
In addition to the acidic group, the organic dye compound of the present invention has a saturated or unsaturated alkyl group having 1 to 20 carbon atoms, an aryol group, a halogen atom, and -OR+.

−N RIR,、−−CON R,Rス、−3O2N 
R,Rz 、 SR,、−−CN 、 −N Oユ、 
N R+CORz、−NR,SO,R2,COOR3(
RI、R2ハ水素N子、炭素数1〜20の飽和または不
飽和アルキル基、アリール基、RJは炭素数1〜20の
飽和または不飽和アルキル基を表す)等の置換基を有し
ていても良い。
-N RIR,,--CON R,RS,-3O2N
R, Rz, SR,, --CN, -N Oyu,
NR+CORz, -NR,SO,R2,COOR3(
RI, R2 has a substituent such as a hydrogen atom, a saturated or unsaturated alkyl group having 1 to 20 carbon atoms, an aryl group, and RJ represents a saturated or unsaturated alkyl group having 1 to 20 carbon atoms. Also good.

また、酸性基は、1価または2価の金属もしくは有機ア
ミン等によって塩を形成していても良い。場合によって
は、アンモニウム塩であってもよい。金属塩の金属とし
てはナトリウム。
Further, the acidic group may form a salt with a monovalent or divalent metal, an organic amine, or the like. In some cases, it may be an ammonium salt. The metal in the metal salt is sodium.

カリウム、マグネシウム、カルシウム、亜鉛。Potassium, magnesium, calcium, zinc.

バリウム、ストロンチウム、マンガン、鉄、ニッケル、
コバルト等である。また、アミン塩のアミンとしては脂
肪族第1級アミン、第2級アミンまたはジアミン等であ
る。
barium, strontium, manganese, iron, nickel,
Cobalt etc. The amine of the amine salt may be an aliphatic primary amine, a secondary amine or a diamine.

本発明の化合物を磁気記録媒体の磁性層中に含有せしめ
るには2本発明に係わる有機色素化合物の少なくとも1
種を水またはトルエン、メチルエチルケトン、あるいは
、シクロヘキサノン等の有機溶媒に溶解し、その溶液に
所定の割合で、磁性粉を浸漬し、攪拌混合した後、濾別
し乾燥処理して得られた処理磁性粉と結着剤を混練する
か、あるいは本発明に係わる有機色素化合物の少なくと
も1種を磁性粉の分散時に直接または適当な溶媒に溶解
して添加しても良い。さらには、磁性塗料の支持体への
塗工前に添加することも可能である。
In order to incorporate the compound of the present invention into the magnetic layer of a magnetic recording medium, at least one of the organic dye compounds according to the present invention may be incorporated.
The treated magnetic powder is obtained by dissolving the seeds in water or an organic solvent such as toluene, methyl ethyl ketone, or cyclohexanone, immersing magnetic powder in the solution at a predetermined ratio, stirring and mixing, filtering and drying. The powder and the binder may be kneaded, or at least one organic dye compound according to the present invention may be added directly or dissolved in a suitable solvent during dispersion of the magnetic powder. Furthermore, it is also possible to add the magnetic coating material before applying it to the support.

本発明の有機色素化合物は2通常、磁性粉に対して0.
1重量%〜20重量%、好ましくは0゜5重量%〜10
重量%の範囲で使用されるのが望ましい。
The organic dye compound of the present invention is usually 0.2 to 0.2 to the magnetic powder.
1% to 20% by weight, preferably 0.5% to 10% by weight
It is desirable to use it within a range of % by weight.

本発明の有機色素化合物を用いて磁性粉および結着剤を
有機溶剤等を用いて混線分散して得られた磁性塗料は1
分散安定性に優れており粘度が低く、さらに、経時のニ
ス分れも少なく。
A magnetic paint obtained by cross-dispersing magnetic powder and a binder using an organic solvent or the like using the organic dye compound of the present invention is 1
It has excellent dispersion stability, low viscosity, and less varnish separation over time.

再度分散性も容易であり、塗工の作業性も著しく優れて
いる。
Again, the dispersibility is easy, and the workability of coating is also extremely excellent.

トをドープしたFe30q、二酸化クロム、バリウムフ
ェライト、または鉄、コバルト等の金属磁性体、あるい
は種々の合金磁性体く例えば、 Fe−Go、 Go−
Ni、 Fe−Co−Ni、 N1−Co−B Fe−
Go−Cr、 Fe−Cr−Ni、 MoB1等)など
が挙げられる。
Fe30q doped with chromium dioxide, barium ferrite, or metal magnetic materials such as iron and cobalt, or various alloy magnetic materials such as Fe-Go, Go-
Ni, Fe-Co-Ni, N1-Co-B Fe-
Go-Cr, Fe-Cr-Ni, MoB1, etc.).

また1本発明に使用しうる結着剤としては特に制限がな
く3例えば前述したような、塩化ビニル−酢酸ビニル共
重合体、塩化ビニル−塩化ビニリデン共重合体、ポリア
クリル酸ブチル。
There are no particular restrictions on the binder that can be used in the present invention, and examples include vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinylidene chloride copolymer, and polybutyl acrylate as described above.

アクリル酸ブチル−アクリロニトリル共重合体、セルロ
ース系樹脂、エポキシ系樹脂、ポリウレタン系樹脂等、
公知の種々の結着剤およびそれらの混合物を使用するこ
とができる。なお。
Butyl acrylate-acrylonitrile copolymer, cellulose resin, epoxy resin, polyurethane resin, etc.
Various known binders and mixtures thereof can be used. In addition.

結着剤としては、熱可塑性型2熱硬化型、電子線硬化型
等いずれのタイプであってもよい。
The binder may be of any type, such as a thermoplastic type, a thermosetting type, or an electron beam curing type.

また1本発明において2本発明の有機色素化合物と、従
来公知の3例えば、レシチン、オキシアミン化合物、ア
ルキルアミン系カチオン界面活性剤、ポリアルキレンソ
ルビタンアルキレート、リン酸エステル等の分散剤ある
いはその他潤滑剤、安定剤等を併用添加することにより
、磁性層の特性を一層高めることが可能である。
In addition, in the present invention, 2 the organic dye compound of the present invention and 3 conventionally known dispersants such as lecithin, oxyamine compounds, alkylamine cationic surfactants, polyalkylene sorbitan alkylates, phosphate esters, or other lubricants. It is possible to further improve the characteristics of the magnetic layer by adding , a stabilizer, etc. in combination.

本発明に係わる磁気記録媒体は、支持体上に、磁性粉、
結合剤、および本発明に係わる有機色素化合物等を有機
溶媒等を用いて混線分散した磁性塗料を塗布乾燥するこ
とによって磁性層を形成したものである。かかる磁性塗
料の製造および塗布法は、従来の方法を適用すれば良く
、また、上記本発明の磁性層には1分散剤、潤滑剤、研
磨剤、帯電防止剤等の添加剤を必要に応じて含有しても
良い。
The magnetic recording medium according to the present invention includes magnetic powder,
A magnetic layer is formed by applying and drying a magnetic paint in which a binder and an organic dye compound according to the present invention are cross-dispersed using an organic solvent or the like. Conventional methods may be used to manufacture and apply such magnetic paints, and additives such as dispersants, lubricants, abrasives, antistatic agents, etc. may be added to the magnetic layer of the present invention as necessary. It may also be contained.

本発明に係わる磁気記録媒体に用いられる支持体として
は、ポリエチレンテレフタレート。
The support used in the magnetic recording medium according to the present invention is polyethylene terephthalate.

ポリエチレンナフタレート、三酢酸セルロース、ポリカ
ーボネート、ポリプロピレン、ポリ塩化ビニル、アルミ
ニウム合金等の任意のものを挙げることができる。
Any material such as polyethylene naphthalate, cellulose triacetate, polycarbonate, polypropylene, polyvinyl chloride, aluminum alloy, etc. can be mentioned.

なお1本発明の磁性層は2通常2μ〜20μの乾燥膜厚
となるように塗設すれば良い。
Note that the magnetic layer of the present invention may be coated so as to have a dry film thickness of usually 2 to 20 microns.

以上1本発明についての説明を、従来の磁気記録媒体と
の相違点を主眼にして行ったが、その他の技術的構成1
例えば、結合剤および必要に応じて用いられる添加剤等
の種類および使用量、さらに支持体の種類や表面平滑化
処理方法、磁性粉の配向方法、塗布の際に用いる有機溶
剤の種類、乾燥方法、硬化方法等については公知の技術
を適用ないし応用すれば良い。
The above description of the present invention has focused on the differences from conventional magnetic recording media, but there are other technical configurations as well.
For example, the type and amount of the binder and additives used as necessary, the type of support, the surface smoothing treatment method, the method of orienting the magnetic powder, the type of organic solvent used during coating, and the drying method. As for the curing method, etc., known techniques may be applied.

以下、実施例および比較例を挙げて本発明を具体的に説
明する。
The present invention will be specifically described below with reference to Examples and Comparative Examples.

実施例1 コバルトをドープしたγ−Feよ0.粉100重量部 塩化ビニル−酢酸ビニル共重合体 7 〃 ウレタンエラストマー 15 〃 本発明に係わる下記有機色素化合物CI)3 〃 トルエン 50 〃 メチルエチルケトン 50 〃 シクロヘキサノン 20 〃 上記組成物をサンドミルを用いて4時間混線分散して磁
性塗料を得た。これを塗料1−Aとする。この塗料1−
Aを15ミクロンのポリエステルフィルム上に塗布乾燥
後、スーパーカレンダーロールにより磁性層の表面処理
加工を行い加熱硬化させた。これを3.81 cmdl
に裁断し実施例2〜29 実施例1において使用した本発明に係わる有機色素化合
物(1)に換えて下記の表1に示す有機色素化合物を使
用した。その他の組成、操作、方法等は実施例1と同様
である。このようにして得られた磁性塗料並びに磁性テ
ープをそれぞれ塗料2−A〜29−A、試料2−B〜2
9−Bとする。
Example 1 γ-Fe doped with cobalt. Powder 100 parts by weight Vinyl chloride-vinyl acetate copolymer 7 Urethane elastomer 15 The following organic dye compound CI) according to the present invention 3 Toluene 50 Methyl ethyl ketone 50 Cyclohexanone 20 The above composition was mixed for 4 hours using a sand mill. A magnetic paint was obtained by dispersing it. This is referred to as paint 1-A. This paint 1-
After coating A on a 15 micron polyester film and drying it, the magnetic layer was surface treated using a super calendar roll and cured by heating. This is 3.81 cmdl
Examples 2 to 29 In place of the organic dye compound (1) according to the present invention used in Example 1, organic dye compounds shown in Table 1 below were used. Other compositions, operations, methods, etc. are the same as in Example 1. The thus obtained magnetic paints and magnetic tapes were used as paints 2-A to 29-A and samples 2-B to 2, respectively.
9-B.

比較例1〜3 実施例1において1本発明に係わる有機色素化合物(1
)を表2に示す如く置き換えて、それぞれ比較例1〜3
とした。
Comparative Examples 1 to 3 In Example 1, one organic dye compound according to the present invention (1
) as shown in Table 2, Comparative Examples 1 to 3, respectively.
And so.

以上の実施例1〜29および比較例1〜3の磁性塗料の
各塗料の特性および磁気テープの各試料の特性を測定し
、それらの結果を表3および表4に示す。
The characteristics of each of the magnetic paints of Examples 1 to 29 and Comparative Examples 1 to 3 and the characteristics of each sample of magnetic tape were measured, and the results are shown in Tables 3 and 4.

表 1 各種有機化合物 表 2 比較添加剤 表 3 磁性塗料の各塗料の特性 (05日後まったくニス分れなし) (05日扱わず力1にニス分れあり) (△2日後ニス分れあり ) (×分散直後ニス分れあり ) 磁性合金(Fe−Go−Ni) 100重量部ポリエス
テル 6 “ ウレタシエラストマ−16〃 実施例21の有機色素化合物 5 〃 トルエン 20 〃 メチルエチルケトン 80 〃 シクロヘキサノン 10 〃 上記組成物を実施例1と同様な方法で混線分散して磁性
塗料を得た。これを塗料30−Aとする。さらにこの磁
性塗料を実施例1と同様に処理して磁気テープを作成し
た。これを試料30−Aとする。
Table 1: Various organic compounds 2: Comparative additives 3: Characteristics of each magnetic paint (no varnish separation at all after 05 days) (varnish separation after 05 days without handling) (varnish separation after 2 days) (× Varnish separated immediately after dispersion) Magnetic alloy (Fe-Go-Ni) 100 parts by weight Polyester 6 "Uretashielastomer-16" Organic dye compound of Example 21 5 Toluene 20 Methyl ethyl ketone 80 Cyclohexanone 10 Above composition A magnetic paint was obtained by cross-dispersing the material in the same manner as in Example 1. This was referred to as paint 30-A. Further, this magnetic paint was treated in the same manner as in Example 1 to create a magnetic tape. is designated as sample 30-A.

実施例31〜58 実施例30において、使用した有機色素化合物に換えて
、下記表5に示す有機色素化合物を使用した。
Examples 31 to 58 In Example 30, organic dye compounds shown in Table 5 below were used in place of the organic dye compounds used.

その他の組成は実施例30と同様であり、また、操作及
び方法等は実施例1と同様にして磁気テープを作成した
。このようにして得られた磁性塗料をそれぞれ塗料31
−A〜58−A。
Other compositions were the same as in Example 30, and a magnetic tape was prepared using the same operations and methods as in Example 1. Each of the magnetic paints obtained in this way was used as paint 31.
-A~58-A.

また、磁気テープをそれぞれ試料31−B〜58−Bと
する。
Further, the magnetic tapes are designated as samples 31-B to 58-B, respectively.

比較例4〜6 実施例30において使用した有機色素化合物を表6に示
す如く置き換えて、それぞれ比較例4〜6とした。
Comparative Examples 4 to 6 Comparative Examples 4 to 6 were prepared by replacing the organic dye compounds used in Example 30 as shown in Table 6.

以上の実施例30〜58および比較例4〜6の磁性塗料
の各塗料の特性および磁気テープの各試料の特性を測定
し、それらの結果を表7および表8に示す。
The characteristics of each of the magnetic paints of Examples 30 to 58 and Comparative Examples 4 to 6 and the characteristics of each sample of magnetic tape were measured, and the results are shown in Tables 7 and 8.

実施例59 コバルトをドープしたFe O粉 100重量部ニトロ
セルロース樹脂 2 〃 ウレタンエラストマー 16 〃 エポキシ樹脂 4 〃 本発明に係わる下記有機色素化合物(n)5 〃 トルエン 45 〃 メチルエヂルケトン 45 〃 シクロヘキサノン 20 〃 上記組成物を実施例1と同様な方法で混線分散した後、
ポリイソシアネート3重量部を添加し、攪拌混合して磁
性塗料を得た。これを、塗料59−Aとする。さらに、
この磁性塗料を実施例1と同様に処理して磁気テープを
作成した。これを試料59−Bとする。
Example 59 Cobalt-doped FeO powder 100 parts by weight Nitrocellulose resin 2 Urethane elastomer 16 Epoxy resin 4 The following organic dye compound (n) according to the present invention 5 Toluene 45 Methyl ethyl ketone 45 Cyclohexanone 20 〃 After cross-dispersing the above composition in the same manner as in Example 1,
3 parts by weight of polyisocyanate was added and mixed with stirring to obtain a magnetic paint. This is referred to as paint 59-A. moreover,
This magnetic paint was treated in the same manner as in Example 1 to produce a magnetic tape. This is designated as sample 59-B.

実施例60〜73 実施例59において使用した本発明に係わる有機色素化
合物(If)に換えて、下記表9に示す有機色素化合物
を使用した。
Examples 60 to 73 In place of the organic dye compound (If) according to the present invention used in Example 59, organic dye compounds shown in Table 9 below were used.

その他の組成は実施例59と同様である。この組成物を
実施例1と同様な方法で混線分散した後、ポリイソシア
ネート3重量部を添加し。
The other compositions are the same as in Example 59. After cross-dispersing this composition in the same manner as in Example 1, 3 parts by weight of polyisocyanate were added.

攪拌混合して磁性塗料を得た。これをそれぞれ塗料60
−A〜73−Aとする。さらにこの磁性塗料を、実施例
1と同様に処理して磁気テープを作成した。これをそれ
ぞれ試料60−B〜73−Bとする。
A magnetic paint was obtained by stirring and mixing. Paint 600 each
-A to 73-A. Further, this magnetic paint was treated in the same manner as in Example 1 to produce a magnetic tape. These are designated as samples 60-B to 73-B, respectively.

比較例7〜9 実施例59において9本発明に係わる有機色素化合物(
If)を表10に示す如く置き換えてそれぞれ比較例7
〜9とシタ。
Comparative Examples 7 to 9 In Example 59, 9 organic dye compounds according to the present invention (
Comparative Example 7 by replacing If) as shown in Table 10.
~9 and sita.

以上の実施例59〜73および比較例7〜9の磁性塗料
の各塗料の特性および磁気テープの各試料の特性を測定
し、それらの結果を表11および表12に示す。
The characteristics of each of the magnetic paints of Examples 59 to 73 and Comparative Examples 7 to 9 and the characteristics of each sample of magnetic tape were measured, and the results are shown in Tables 11 and 12.

表 9 表 10 表 12 実施例74〜76 実施例1において、使用した本発明に係わる有機色素化
合物(1)に換えて2表13の如〈従来公知の分散剤と
2本発明に係わる有機色素化合物を併用添加した。その
他の組成、操作。
Table 9 Table 10 Table 12 Examples 74 to 76 In Example 1, in place of the organic dye compound (1) according to the present invention used, 2 as shown in Table 13 (conventionally known dispersant and 2 organic pigments according to the present invention) were used. Compounds were added in combination. Other compositions, operations.

方法等は実施例1と同様である。このようにして得られ
た磁気テープをそれぞれ試料74−B〜76−Bとする
The method and the like are the same as in Example 1. The magnetic tapes thus obtained are designated as samples 74-B to 76-B, respectively.

以上の実施例74〜76の磁気テープの各試料の特性を
測定し、それらの結果を表14に示す。
The characteristics of each sample of the magnetic tape of Examples 74 to 76 above were measured, and the results are shown in Table 14.

Claims (1)

【特許請求の範囲】 1、磁性粉および結着剤を含む磁性層を支持体上に形成
して成る磁気記録媒体において、磁性層に、酸性基また
はその塩を有する有機色素化合物を含有せしめてなるこ
とを特徴とする磁気記録媒体。 2、水酸基、カルボキシル基、スルホン酸基ならびにこ
れらの1価もしくは2価の金属塩またはアミン塩から選
ばれる少なくとも1種以上の酸性基またはその塩を有す
る有機色素化合物を磁性層に含有せしめてなる特許請求
の範囲第1項記載の、磁気記録媒体。
[Claims] 1. A magnetic recording medium comprising a magnetic layer containing magnetic powder and a binder formed on a support, wherein the magnetic layer contains an organic dye compound having an acidic group or a salt thereof. A magnetic recording medium characterized by: 2. The magnetic layer contains an organic dye compound having at least one or more acidic groups selected from hydroxyl groups, carboxyl groups, sulfonic acid groups, and monovalent or divalent metal salts or amine salts thereof, or salts thereof. A magnetic recording medium according to claim 1.
JP58205946A 1983-11-04 1983-11-04 Magnetic recording medium Granted JPS6098525A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58205946A JPS6098525A (en) 1983-11-04 1983-11-04 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58205946A JPS6098525A (en) 1983-11-04 1983-11-04 Magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS6098525A true JPS6098525A (en) 1985-06-01
JPH0262893B2 JPH0262893B2 (en) 1990-12-26

Family

ID=16515327

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58205946A Granted JPS6098525A (en) 1983-11-04 1983-11-04 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS6098525A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61261817A (en) * 1985-05-15 1986-11-19 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS61261818A (en) * 1985-05-15 1986-11-19 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623430A (en) * 1985-06-27 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623432A (en) * 1985-06-28 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623429A (en) * 1985-06-28 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS62119725A (en) * 1985-11-19 1987-06-01 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS62134824A (en) * 1985-12-07 1987-06-17 Konishiroku Photo Ind Co Ltd Magnetic recording medium
US5514465A (en) * 1993-06-30 1996-05-07 Tdk Corporation Magnetic recording medium comprising a magnetic layer containing magnetic powder, an organic dye and a binder having an amino group or ammonium salt group

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI491676B (en) 2010-06-01 2015-07-11 Fujifilm Corp Pigment dispersion composition, red colored composition, colored curable composition, color filter for a solid state imaging device and method for producing the same, and solid state imaging device

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61261817A (en) * 1985-05-15 1986-11-19 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS61261818A (en) * 1985-05-15 1986-11-19 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623430A (en) * 1985-06-27 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623432A (en) * 1985-06-28 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS623429A (en) * 1985-06-28 1987-01-09 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS62119725A (en) * 1985-11-19 1987-06-01 Konishiroku Photo Ind Co Ltd Magnetic recording medium
JPS62134824A (en) * 1985-12-07 1987-06-17 Konishiroku Photo Ind Co Ltd Magnetic recording medium
US5514465A (en) * 1993-06-30 1996-05-07 Tdk Corporation Magnetic recording medium comprising a magnetic layer containing magnetic powder, an organic dye and a binder having an amino group or ammonium salt group

Also Published As

Publication number Publication date
JPH0262893B2 (en) 1990-12-26

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